Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
  • C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
  • C09B67/008—Preparations of disperse dyes or solvent dyes
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
  • C09B23/14—Styryl dyes
  • C09B23/143—Styryl dyes the ethylene chain carrying a COOH or a functionally modified derivative, e.g.-CN, -COR, -COOR, -CON=, C6H5-CH=C-CN
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B56/00—Azo dyes containing other chromophoric systems
  • C09B56/08—Styryl-azo dyes

Definitions

• the present invention relates to disperse dyes, to the preparation thereof and to the use thereof for dyeing synthetic organic material.
• the dyes according to the invention conform to the formula ##STR4## in which X is hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy or halogen, Y is hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkyl or C 1 -C 4 alkoxy-C 1 -C 4 alkoxy, R is hydrogen, C 1 -C 12 alkyl, C 2 -C 12 alkenyl or phenyl, or Y and R, together with the nitrogen atom and the two C atoms linking them, form a 5- or 6-ring, B is a straight-chain or branched C 2 -C 6 alkylene radical, Z is a bridge member of the formula ##STR5## or a direct bond and A is a radical of the formula ##STR6## which radicals
• alkyl groups as used in this application is generally to be understood as meaning straight-chain, branched or cyclic alkyl groups. They comprise for example methyl, ethyl, propyl, i-propyl, butyl, i-butyl, tert-butyl, amyl, tert-amyl (1,1-dimethylpropyl), 1,1,3,3-tetramethylbutyl, hexyl, 1-methylpentyl, neopentyl, 1-, 2- or 3-methyl-hexyl, heptyl, n-octyl, tert-octyl, 2-ethylhexyl, n-nonyl, isononyl, decyl, dodecyl, cyclopentyl, cyclohexyl, methylcyclohexyl and the associated isomers.
• alkyl radicals may be substituted, for example by hydroxyl, alkoxy, having 1 to 4 carbon atoms, in particular methoxy, cyano or phenyl.
• Suitable other substituents are halogen, such as fluorine, chlorine or bromine, and -CO-U, in which U is alkyl having 1 to 6 carbon atoms or phenyl.
• Suitable alkenyl radicals are those radicals which are derived from the above mentioned alkyl radicals by replacement of at least one single bond by a double bond. Suitable radicals are for example ethenyl and propenyl.
• Suitable alkoxy radicals are for example methoxy, ethoxy, propoxy, isopropoxy, n-butoxy, i-butoxy and tert-butoxy.
• Suitable substituted alkyl radicals are: methoxymethyl, ethoxymethyl, ethoxyethyl, ethoxypropyl, n-propoxymethyl, iso-propoxymethyl, butoxymethyl, butoxyethyl, butoxypropyl, ethoxypentyl, methoxybutyl, ethoxypentyl, 2-hydroxyethoxypentyl, cyanoethyl and hydroxyethyl.
• alkylene radicals B can likewise be straight-chain or branched or even substituted. Possibilities are for example ethylene, 1,3-propylene, 1,2-propylene, 1,2-butylene, 1,6-hexylene, 2-hydroxy-1,3-propylene and 2-chloro-1,3-propylene.
• phenyl radicals as used in this application is generally to be understood as meaning unsubstituted or substituted phenyl radicals. Possible substituents are for example C 1 -C 4 alkyl, C 1 -C 4 alkoxy, bromine, chlorine, nitro and C 1 -C 4 alkylcarbonylamino.
• halogen as used in this application is generally to be understood as meaning fluorine, bromine and in particular chlorine.
• Z is a direct bond or a bridge member from the series --O--, --S--, --NH--, ##STR7## are preferred if the bond to the radical A is via a carbon atom of this radical. If the radical A has a hetero atom via which the bond to the rest of the dye molecule of the formula (1) is established, Z is preferably a direct bond.
• radicals A are the radicals of the formulae ##STR8## These radicals can additionally bear the substituents customery with disperse dyes, for example C 1 -C 4 alkyl, C 1 -C 4 alkoxy, halogen or nitro.
• X are hydrogen, methyl, methoxy, chlorine and bromine, particular preference being given to hydrogen and methyl.
• Y is preferably chlorine, methyl, methoxy, methoxyethyl or methoxyethoxy and in particular hydrogen.
• R is C 1 -C 4 alkyl, which can be substituted by hydroxyl, C 1 -C 4 alkoxy or phenyl.
• R is methyl, ethyl or benzyl.
• R and Y can combine with the nitrogen atom and the two C atoms joining them to form a 5- or 6-membered ring which can contain an oxygen atom as a further hetero atom. Suitable substituents for these rings are for example hydroxyl, methyl, methoxy, chlorine and phenyl.
• R and Y together with the nitrogen atom and the two C atoms joining them form a 6-ring which is unsubstituted or bears 1 to 3 methyl groups.
• B is preferably a straight-chain or branched alkylene radical having 2 to 4 carbon atoms which can be substituted by hydroxyl. Particular preference is given to the disperse dyes of the formula (1) in which B is ethylene or 1,3-propylene.
• a 1 is a radical of the formula ##STR11##
• the compounds of the formula (1) are prepared in a manner known per se, for example by reacting a compound of the formula ##STR12## with tetracyanoethylene, or by reacting a compound of the formula ##STR13## with a cyanide and then with an oxidizing agent.
• the compounds of the formulae (3) and (4) are known or can be obtained in a manner known per se.
• the compounds of the formula (3) can be obtained for example by reacting a compound of the formula
• A, Z, B, X, Y and R are as defined under the formula (1) and Hal is chlorine or bromine, it being possible for the two halogen atoms to be identical or different.
• the compounds of the formulae (7) and (8) are known or can be prepared in a manner known per se.
• the reaction of the compound (7) with the compound (8) is preferably carried out in an inert organic solvent and in the presence of a base.
• Suitable inert organic solvents are for example compounds having a boiling point above 100° C., such as alcohols, ethers, esters, nitrobenzene, halobenzene, toluene, xylenes and the like.
• Suitable are in particular higher-boiling alcohols, such as tert-butanol, and also ethers of polyvalent alcohols, for example diethylene glycol monoethyl ether or monomethyl ether, and also the corresponding diethers.
• the components (7) and (8) can be used in a stoichiometric ratio, or very frequently an excess of one of the components, preferably compound (8), will prove to be favourable.
• the reaction temperature is between about 80° and 150° C., preferably between 100° and 130° C., and the reaction time range extends from about 1 hour to 20 hours, depending on the temperature and the reactants.
• component (8) which may have been used in excess, is removed, and the compound of the formula (5) obtained is then reacted with an aniline derivative of the formula (6).
• This reaction is preferably carried out in one of the above-mentioned solvents.
• the temperature is normally above 100° C., in particular between 120° and 200° C., especially between 140° and 180° C.
• the components (5) and (6) can be used in a stoichiometric ratio, although normally the more readily accessible component, usually the aniline derivative (6), will be used in excess, for example in an excess of 10%.
• reaction mixture is worked up in a conventional manner, for example by removing the excess of component (6) and the solvent and purifying the residue if necessary, for example by recrystallization.
• Both the reaction of compounds (7) and (8) and the reaction of compounds (5) and (6) are carried out in the presence of a base, not only organic but also inorganic bases being suitable, for example pyridine, piperidine, triethylamine, sodium carbonate, potassium carbonate, sodium hydrogencarbonate or potassium hydrogencarbonate.
• a base not only organic but also inorganic bases being suitable, for example pyridine, piperidine, triethylamine, sodium carbonate, potassium carbonate, sodium hydrogencarbonate or potassium hydrogencarbonate.
• This base is generally used in a small excess, for example in an excess of 10%.
• the whole preparation of compound (3) can also be carried out as a one-pot reaction in that the same solvent is used for both reaction steps and compound (5) is not isolated.
• the compounds of the formula (4) are obtained for example by first reacting a compound of the formula (3) under the known conditions of the Vilsmeier synthesis with, for example, POCl 3 and dimethylformamide or phosgene and dimethylformamide and then reacting the product with malodinitrile.
• reaction of compounds of the formula (3) with tetracyanoethylene is carried out in a manner known per se, preferably in an inert solvent at a temperature between about 20° and 100° C., the reaction components being used in substantially equivalent amounts.
• reaction of the compounds of the formula (4) with a cyanide and then with an oxidizing agent is carried out in a manner known per se.
• the reaction is carried out as a one-pot reaction, i.e. without isolation of the intermediate, and likewise in an inert solvent.
• the cyanide used is in particular potassium cyanide or sodium cyanide, and the oxidizing agent used is in particular bromine.
• the reaction with the cyanide is preferably carried out at about 20° to 100° C. and the reaction with the oxidizing agent at about 0° to 20° C.
• Suitable inert solvents for the preceding reactions are for example halogen compounds, such as chloroform or chlorobenzene, ethers, aromatic compounds, such as benzene, toluene or xylene, but in particular tetrahydrofuran or dimethylformamide.
• the dyes of the foraula (1) are isolated for example by pouring the reaction solutions into ice-water, after which the precipitated dye is filtered off, possibly washed and dried.
• the compounds of the formula (1) according to the invention can be used as dyes for dyeing and printing cellulosic and in particular synthetic hydrophobic fibre materials, in particular textile materials. Textile materials composed of blend fabrics which contain such cellulosic or synthetic hydrophobic textile materials can likewise be dyed or printed with the compounds according to the invention.
• Suitable cellulosic textile materials are in particular secondary cellulose acetate and cellulose triacetate.
• Synthetic hydrophobic textile materials consist in particular of linear, aromatic polyesters, for example those of terephthalic acid and glycols, in particular ethylene glycol or condensation products of terephthalic acid and 1,4-bis(hydroxymethyl)cyclohexane, or polycarbonates, for example those of ⁇ , ⁇ -dimethyl-4,4'-dihydroxy-diphenylmethane and phosgene, or fibres on a polyvinyl chloride or polyamide basis.
• polyester fibre materials are dyed from an aqueous dispersion by the exhaust method i..n the presence of customary anionic or nonionic dispersants and in the presence or absence of customary swelling agents (carriers) at temperatures between 80° and 140° C.
• Secondary cellulose acetate is preferably dyed at around 65° to 85° C. and cellulose triacetate at temperatures up to 115° C.
• novel dyes produce little or no staining on wool and cotton present in the dyebath at the same time (thus exhibiting very good reserve), so that they can also be efficiently used for dyeing polyester/wool and polyester/cellulose fibres blend fabrics.
• the dyes according to the invention are suitable in particular for dyeing by the thermosol process.
• the textile material mentioned can be present in a wide variety of processing forms, for example as fibre, yarn or web or as woven or knitted fabric.
• the dye is ground so that its average particle size is between 0.01 and 10 microns.
• the grinding can be carried out in the presence of dispersants.
• the dried dye is ground together with a dispersant or kneaded in paste form together with a dispersant and then dried in vacuo or by atomizing.
• the preparations thus obtained can be used for dyeing and printing.
• the customary thickeners are used, for example modified or unmodified natural products, for example alginates, british gum, gum arabic, crystal gum, locust bean ether gum, tragacanth, carboxymethylcellulose, hydroxyethylcellulose, starch or synthetic products, for example polyacrylamide, polyacrylic acid or copolymers of polyvinyl alcohol.
• modified or unmodified natural products for example alginates, british gum, gum arabic, crystal gum, locust bean ether gum, tragacanth, carboxymethylcellulose, hydroxyethylcellulose, starch or synthetic products, for example polyacrylamide, polyacrylic acid or copolymers of polyvinyl alcohol.
• the dyes according to the invention confer on the materials mentioned, in particular on polyester material, level orange or red shades having very good performance-fastness properties, in particular good light fastness, fastness to dry heat pleating and setting, chlorinated water and wet fastness such as water, perspiration and wash fastness; the dyeings are further typified by good pH stability and very good rub fastness. The dyeings are also very strong in color. Of particular note is the good thermomigration fastness of the dyeings obtained.
• the dyes according to the invention are also efficiently usable for Producing mixed shades together with other dyes. It is of course also possible to use mixtures of the dyes according to the invention with one another.
• the aforementioned use of the azo compounds of the formula (1) according to the invention forms part of the subject-matter of the present invention just as much as a process for dyeing or printing cellulosic or synthetic hydrophobic fibre material, in particular textile material, which comprises applying or incorporating one or more compounds of the formula (1) to or in the material mentioned.
• the hydrophobic fibre material mentioned is preferably textile polyester material.
• the present invention further provides the hydrophobic fibre material, preferably polyester textile material, dyed or printed by the process mentioned.
• a solution of 17.2 g of the compound of the formula ##STR18## in 60 ml of dimethylformamide is admixed in the course of about 7 minutes with 7.5 g of tetracyanoethylene added a little at a time.
• the solution immediately turns red and heats up to about 36°. Heating is applied to raise the temperature further to 55°-60°. After about 10 minutes a thin layer chromatogram no longer shows any starting material.
• the reaction mixture is discharged onto 500 ml of ice-water, and the sticky dye is filtered off on a nutsche filter, washed with water and then, to remove excess tetracyanoethylene, with 20 % sodium sulfite solution and finally again with water.
• the starting compound is prepared as follows: 19.8 g of 4-hydroxyazobenzene are dissolved in 100 ml of diethylene glycol monoethyl ether, and the solution is admixed with 12.8 g of sodium carbonate and 52.5 ml of 1,2-dibromoethane. The mixture is then heated to about 116° C. and stirred at that temperature for 2 hours. The excess dibromoethane is then removed by steam distillation and thereafter the water by distillation at about 110° C. in vacuo.
• Example 1 1 part of dry, extender-free dye of Example 1 is mixed in a sand mill together with 2 parts of dinaphthylmethanedilsulfonate (Na salt), 34 parts of quartz sand and 17 parts of water, and the mixture is ground until a particle size of about 2 3/4 or less is obtained.
• the suspension formed is separated from the sand to leave a stable liquid formulation.
• the suspension can also be subjected to spray drying, in which case a pulverulent dyeing preparation is obtained.
• Polyethylene terephthalate fabric is impregnated on a padmangle at 40° with a liquor of the following composition:
• the fabric is squeezed off to about 60%, dried at 100° and then set at a temperature of 210° for 60 seconds.
• the dyed fabric is washed with water, soaped off or reduction-cleared and dried.
• the result obtained is a brilliant, lightfast red dyeing which is distinguished in particular by good thermomigration fastness.
• the dyeing is subsequently rinsed and aftertreated with aqueous sodium hydroxide solution and a dispersant to give a red dyeing which is fast to light and sublimation.
• This dye preparation is stirred up with 40 parts of a 10% aqueous solution of the sodium salt of N-benzylheptadecylbenzimidazoledisulfonic acid and admixed with 4 parts of a 40% acetic acid solution.
• a dyebath is prepared therefrom by diluting with water to 4,000 parts.
• This bath is then entered at 50° with 100 parts of a polyester fibre material, the temperature is raised to 120° to 130° in the course of halfan hour, and dyeing is carried out at that temperature in a sealed vessel for one hour. This is followed by thorough rinsing to leave a ruby red dyeing having good fastness properties, in particular good sublimation and thermomigration fastness.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Coloring (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Inks, Pencil-Leads, Or Crayons (AREA)
• Optical Filters (AREA)

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Citations (18)

• 1988
  • 1988-03-11 US US07/166,944 patent/US4914190A/en not_active Expired - Fee Related
  • 1988-03-14 EP EP88810156A patent/EP0284560B1/fr not_active Expired - Lifetime
  • 1988-03-14 DE DE8888810156T patent/DE3868656D1/de not_active Expired - Lifetime
  • 1988-03-17 JP JP63062076A patent/JPS63254168A/ja active Pending
  • 1988-03-18 KR KR1019880002859A patent/KR880011287A/ko not_active Withdrawn

Patent Citations (18)

Non-Patent Citations (3)

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